Determine the necessary mass, volume, or concentration for preparing a solution.
≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Cyclopentanemethanol was used to study catalytic reduction of 6-bromo-1-hexene by nickel (I) salen electrogenerated at a glassy carbon electrode in acetonitrile containing tetramethylammonium tetrafluoroborate by cyclic voltammetry and controlled-potential electrolysis.
| Canonical Smiles | C1CCC(C1)CO |
|---|---|
| IUPAC Name | cyclopentylmethanol |
| InChIKey | ISQVBYGGNVVVHB-UHFFFAOYSA-N |
| INCHI | 1S/C6H12O/c7-5-6-3-1-2-4-6/h6-7H,1-5H2 |
| Isomeric SMILES | C1CCC(C1)CO |
| WGK Germany | 3 |
| Molecular Weight | 100.16 |
| Beilstein | 1919000 |
| Reaxy-Rn | 1919000 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1919000&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Primary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Hydrocarbon derivative - Primary alcohol - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 10, 2025 | C742604 |
| Sensitivity | Air sensitive |
|---|---|
| Refractive Index | 1.458 |
| Flash Point(°F) | 143.6 °F |
| Flash Point(°C) | 62°C |
| Boil Point(°C) | 162-163°C |
| Molecular Weight | 100.160 g/mol |
| XLogP3 | 1.400 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 100.089 Da |
| Monoisotopic Mass | 100.089 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 46.100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Luyao Guo, Xiaoyan Liu, Ziang Zhao, Ronghe Lin, Yu Meng, Xinzheng Ma, Yihui Li, Xiaoling Mou, Li Yan, Hejun Zhu, Yunjie Ding. (2023) Nanostructured PtBi Alloy Enables Direct Oxidation of Linear α-Alcohols to Fatty Acids. ACS Catalysis, [PMID:] [10.1021/acscatal.3c03458] |